A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date1995/01/16
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Indian UGC (journal)
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Refrences60
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Citations62
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Bernhard Kräutler
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Josef Maynollo
Cite
Kräutler, Bernhard, and Josef Maynollo. “A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60”. Angewandte Chemie International Edition in English, vol. 34, no. 1, 1995, pp. 87-88, https://doi.org/10.1002/anie.199500871.
Kräutler, B., & Maynollo, J. (1995). A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60. Angewandte Chemie International Edition in English, 34(1), 87-88. https://doi.org/10.1002/anie.199500871
Kräutler, Bernhard, and Josef Maynollo. “A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60”. Angewandte Chemie International Edition in English 34, no. 1 (1995): 87-88. https://doi.org/10.1002/anie.199500871.
Kräutler B, Maynollo J. A Highly Symmetric Sixfold Cycloaddition Product of Fullerene C60. Angewandte Chemie International Edition in English. 1995;34(1):87-8.
Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
C70 ist stabiler als C60: experimentelle Bestimmung der Bildungswärme von C70 | Angewandte Chemie | 12 | 1994 | |
| C70 ist stabiler als C60: experimentelle Bestimmung der Bildungswärme von C70 | Scientific American |
| 1991 | |
| C70 ist stabiler als C60: experimentelle Bestimmung der Bildungswärme von C70 | Chemie in unserer Zeit |
| 1994 | |
| C70 ist stabiler als C60: experimentelle Bestimmung der Bildungswärme von C70 | 1993 | |||
| Formation and stabilisation of the hexa-cyclopentadiene adduct of C60 | Journal of the Chemical Society, Chemical Communications | 33 | 1993 |
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Extending on-surface synthesis from 2D to 3D by cycloaddition with C60 | Nature Communications |
| 2023 | |
The intermolecular anthracene-transfer in a regiospecific antipodal C60difunctionalization | Organic & Biomolecular Chemistry |
| 2020 | |
An Elusive Nonaromatic Goal behind the Centropolyindanes: Aufbau of Veratrolo‐Annelated Centropolyquinanes and Ozonolytic Abbau | ChemPlusChem |
| 9 | 2017 |
| Regiochemically Controlled Synthesis of a β-4-β′ [70]Fullerene Bis-Adduct | The Journal of Organic Chemistry |
| 6 | 2017 |
Recent progress in the synthesis of regio‐isomerically pure bis‐adducts of empty and endohedral fullerenes | Journal of Physical Organic Chemistry |
| 23 | 2016 |
Citations Analysis
The category
Science: Chemistry 43
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled Hetero-diels-alder reaction of fullerene: Synthesis of thiochroman-fused C60 with o-thioquinone methide and oxidation to its S-oxides and was published in 1995. The most recent citation comes from a 2023 study titled Extending on-surface synthesis from 2D to 3D by cycloaddition with C60. This article reached its peak citation in 1996, with 13 citations. It has been cited in 31 different journals, 6% of which are open access. Among related journals, the The Journal of Organic Chemistry cited this research the most, with 6 citations. The chart below illustrates the annual citation trends for this article.